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Endometriosis

GREB1 · rs13394619

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Endometriosis — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2012, PMID:23104006)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Endometriosis. (GWAS Catalog, Nat Genet 2012, PMID:23104006)
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Endometriosis compared to the general population. (GWAS Catalog, Nat Genet 2012, PMID:23104006)

Source: GWAS Catalog, Nat Genet 2012, PMID:23104006

What people read about alongside this

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs13394619

What is rs13394619?

rs13394619 is a single position in the genome, in or near the GREB1 gene. Published research associates it with endometriosis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What do people read about alongside rs13394619?

Subjects that appear in the title or abstract of the same papers as this rsID include fertility (2 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs13394619 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs13394619 come from?

GWAS Catalog, Nat Genet 2012, PMID:23104006. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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